Polypropylene Chemical Properties

Melting point:

157 °C

Boiling point:

120-132 °C

Density 

0.9 g/mL at 25 °C (lit.)

refractive index 

n20/D 1.49(lit.)

Flash point:

>470

storage temp. 

-20°C

form 

particles (Spherical)

Odor

odorless

Merck 

13,7663

Dielectric constant

1.5（Ambient）

NIST Chemistry Reference

Polypropylene, atactic(9003-07-0)

IARC

3 (Vol. 19, Sup 7) 1987

EPA Substance Registry System

Polypropylene (9003-07-0)

Safety Information

WGK Germany 

3

RTECS 

UD1842000

TSCA 

Yes

HS Code 

39021000

Hazardous Substances Data

9003-07-0(Hazardous Substances Data)

Toxicity

LD50 intraperitoneal in rat: > 110gm/kg

MSDS

• Language:English Provider:Polypropylene
• Language:English Provider:SigmaAldrich

Polypropylene Usage And Synthesis

Chemical Properties

Translucent, white solid.Tensile strength 5000 psi, flexural strength 7000 psi, usable up to 121C. Insoluble in cold organic solvents; softened by hot solvents. Maintains strength after repeated flexing. Degraded by heat and light unless protected by antioxidants. Readily colored; good electrical resistance; low water absorption and moisture permeability; poor impact strength below ?9.4C; not attacked by fungi or bacteria; resists strong acids and alkalies up to 60C, but is attacked by chlorine, fuming nitric acid, and other strong oxidizing agents. Combustible, but slow-burning. Fair abrasion and good heat resis- tance if properly modified. Can be chrome-plated, injectionand blow-molded, and extruded.

Chemical Properties

Polypropylene is a low-density resin that offers a good balance of thermal, chemical, and electrical properties, along with moderate strength. Strength can be significantly increased by using reinforcing agents such as glass fiber. Polypropylene has limited heat resistance, but it can be used in applications that must withstand boiling water or steam sterilization.
Polypropylenes can resist chemical attack and are unaffected by aqueous solutions of inorganic salts or mineral acids and bases, even at high temperatures. They are not attacked by most organic chemicals, and there is no solvent for these resins at room temperature. The resins are attacked, however, by halogens, fuming nitric acid, other active oxidizing agents, and by aromatic and chlorinated hydrocarbons at high temperatures .
Polypropylene is translucent and autoclavable. Properties can be improved by compounding with fillers, by blending with synthetic elastomers, and by copolymerizing with small amounts of other monomers.

Uses

Polypropylene (PP) is a thermoplastic material used in a wide variety of applications including packaging, labeling, textiles, etc. Due to high processability and low cost, PP is one of the most extensively produced polymers, especially, for auto industry. Pristine PP is resistant to photo-oxidation and thermal oxidation at moderate temperatures. However, PP is sensitive to various external aging environments (such as heat, light, and radiation), and, hence, has a relatively low service temperature.When PP is exposed to high temperatures or to an irradiation environment, the tertiary hydrogen atoms present in PP chains are susceptible to be attacked by oxygen. It is well known that PP oxidation depends on both light and temperature in outdoor aging conditions. PP can also be photo-degraded because several molecular chains are affected in the wavelength range from 310 to 350 nm.

Uses

Used with ram- and screw-injection machines. For automotive, housewares, general molding products and multi- and monofiliment fiber.

Uses

General extrusion grade polymer.

Uses

Base polymer in hot melt adhesives and paper-laminating, extender and viscosity modifier in caulks and sealants and waterproofing agent in wire and cable applications.

Uses

Modifier for waxes to reduce blocking, scuffing and abrasion. Improves pigment dispersion in polypropylene films and fibers.

Definition

ChEBI: A polymer compose of repeating propane-1,2-diyl units.

Definition

polypropylene: Anisotactic polymer existing in bothlow and high formula-weight forms.The lower-formula-weight polymer ismade by passing propene at moderatepressure over a heated phosphoricacid catalyst spread on aninert material at 200°C. The reactionyields the trimer and tetramer. Thehigher-formula-weight polymer isproduced by passing propene into aninert solvent, heptane, which containsa trialkyl aluminium and a titaniumcompound. The product is amixture of isotactic and atacticpolypropene, the former being themajor constituent. Polypropene isused as a thermoplastic mouldingmaterial.

Production Methods

In PP production, propylene monomer is polymerized to make the homopolymer by using a Ziegler–Natta type coordination catalyst. This catalyst results from the reaction and interaction of a transition metal compound and an organometallic compound, usually an alkylaluminum compound. Halide atoms are involved in most such catalyst systems .
Polypropylene can be made by solution, slurry (or solvent), bulk (or liquid propylene), or gas-phase polymerization, or a combination of these processes . The most widely used is the slurry process; however, the current trend is toward the gas-phase process. In the solution, slurry, and bulk processes, the catalyst system is mixed with propylene and a hydrocarbon diluent (usually hexane, heptane, or liquid propylene) in a reactor. After polymerization, the reaction mixture enters a flash tank where unreacted propylene is removed and recycled. Propylene–ethylene copolymers [9010-79-1] can be manufactured when ethylene is fed along with propylene to the polymerization reactor or by adding ethylene and propylene to a postpolymerization reactor that contains PP. This mixture may then be purified to remove lowmolecular weight and atactic fractions and washed to remove catalyst residues. The polypropylene resin is then dried and pelletized. During this time, additivesmay be incorporated in the gas-phase process; no liquid diluent is used .

Preparation

High pressure, free radical processes of the type used to prepare polyethylene are not satisfactory when applied to propylene and other tX-olefins bearing a hydrogen atom on the carbon atom adjacent to the double bond. This is attributed to extensive transfer of this hydrogen to propagating centres (R .):

The resulting allyl radical is resonance stabilized and has a reduced tendency to react with another monomer molecule.
Although the Phillips and Standard Oil processes can be used to prepare polypropylene, the polymer yields tend to be low and it appears that these processes have not been used for commercial production of polypropylene. Until about 1980, polypropylene has been produced commercially only by the use of Ziegler-Natta catalysts. Commonly a slurry process is used and is carried out in much the same manner as described previously for the preparation of polyethylene ). In the case of polypropylene, some atactic polymer is formed besides the required isotactic polymer; but much of this atactic material is soluble in the diluent (commonly heptane) so that the product isolated is largely isotactic polymer. Recently, there has been a marked shift towards processes involving gas phase polymerization and liquid phase polymerization. Few details of these newer processes have been published. Gas phase processes resemble those described previously for the preparation of polyethylene ) and swing plants are now feasible. In liquid phase processes polymerization is conducted in liquid propylene, typically at 2 MPa (20 atmospheres) and 55??C. Concurrently with these developments, new catalyst systems have been introduced. These materials have very high activity and the reduced levels that are required make it unnecessary to remove catalyst from the final polymer. Also, the new catalyst systems lead to polypropylene with higher'proportions of isotactic polymer and removal of atactic polymer is not necessary.

General Description

Tan to white odorless solid. Less dense than water and insoluble in water. Hence floats on water.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Polypropylene reacts with chlorine, fuming nitric acid and other strong oxidizing agents.

Hazard

Questionable carcinogen.

Health Hazard

No apparent toxicity

Industrial uses

Polypropylene is similar in structure to polyethylene,but every other carbon atom has oneof its H2 atoms replaced by a CH2group.Although electrically similar to polyethylene,polypropylene can be made in thinner films, say 5μm as against about 25 μm for polyethylene.These films replace paper for impregnatedcapacitors, with reduced loss.

Safety Profile

Moderately toxic by ingestion and intraperitoneal routes. Questionable carcinogen. When heated to decomposition it emits acrid smoke and irritating fumes. Used in injection molding for auto parts, in bottle caps, and in container closures.

Carcinogenicity

No data on the carcinogenicity and mutagenicity of propylene are available for evaluation by the working group.

Solubility in organics

Chlorinated hydrocarbons, diethyl ether, hydrocarbons, isoamyl acetate, toluene; Insoluble in more polar organic solvents with small hydrocarbon groups even at elevated temperatures

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